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nsv5695888

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Description:Insertion of a Alu mobile element relative to the reference
  • Publication(s):Chuang et al. 2021

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 163 SVs from 38 studies. See in: genome view    
Submitted genomic56,627,048-56,627,048Question Mark
Overlapping variant regions from other studies: 163 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):56,660,960-56,660,960Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5695888Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1656,627,04856,627,048
nsv5695888RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1656,660,96056,660,960

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17198808alu insertionSequencingOther
nssv17217781alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17198808Submitted genomicNC_000016.10:g.566
27048_56627049ins2
80
GRCh38 (hg38)NC_000016.10Chr1656,627,04856,627,048
nssv17217781Submitted genomicNC_000016.10:g.566
27048_56627049ins2
80
GRCh38 (hg38)NC_000016.10Chr1656,627,04856,627,048
nssv17198808RemappedPerfectNC_000016.9:g.5666
0960_56660961ins28
0
GRCh37.p13First PassNC_000016.9Chr1656,660,96056,660,960
nssv17217781RemappedPerfectNC_000016.9:g.5666
0960_56660961ins28
0
GRCh37.p13First PassNC_000016.9Chr1656,660,96056,660,960

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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